#FoundationForward
In 1997, Bob Rosen was diagnosed with PV — and found no roadmap. So, he built one. 

25 years later, we’re moving #FoundationForward, empowering patients with research, resources, and support. 

📥 Join our community: https://goto.mpnresearchfoundation.org/425ellc
 #MPNResearch #RareDisease
May 25, 2025 at 3:01 PM
Holochain Horizon: Foundation Forward is live! Read the recap of our first livestream and learn about The Holochain Foundation's strategic shift to a more proactive role. blog.holochain.org/holochain-ho...
#Holochain #DecentralizedTech #FoundationForward
August 15, 2025 at 4:26 PM
“Scientific progress is almost always interconnected, and breakthroughs in one area frequently ripple across others.” -Dr. Vijay Sankaran 
Support collaboration. Move #FoundationForward. 

Join our community: https://goto.mpnresearchfoundation.org/425ellc 
#MPNResearch #RareDisease
May 12, 2025 at 2:02 AM
Support #MPNresearch the fun way: 
 - Buy #KrispyKreme Digital Dozens https://f.mtr.cool/xxljcncihc
 - Come to Angels vs. Marlins on May 23 https://f.mtr.cool/czmkcgszao

Each #donut + #ticket fuels our mission to move #FoundationForward  
#MPNResearch #FundraisingFun
May 10, 2025 at 3:30 PM
Thank you to everyone who donated to #FoundationForward — you're powering patient-driven research and honoring Bob Rosen’s legacy. 

⏳ Today’s the last day to give. 

Let’s finish strong. 
📥 Donate now: https://goto.mpnresearchfoundation.org/4js24x1 

#MPNResearch #RareDisease #LastDayToGive
May 31, 2025 at 3:02 PM
25 yrs ago, MPNs had no research roadmap.

Then came Bob Rosen.

His first grant helped lead to the discovery of JAK2 in 2005 — a breakthrough that changed everything.

We're moving #FoundationForward.
Join us: https://goto.mpnresearchfoundation.org/425ellc

#MPNResearch #RareDisease #BobRosenLegacy
May 30, 2025 at 3:02 PM
72% of MPN patients are unaware of the MPN 10 symptom-tracking tool. 

We're moving #FoundationForward by raising awareness. 
💬 Ever used it? Heard of it? Tell us below! 

📥 Subscribe for updates: https://mpnresearchfoundation.org/subscribe-to-our-newsletter/
#MPNResearch #RareDisease
May 28, 2025 at 2:02 PM
MPNs don’t appear overnight — mutations like JAK2 V617F can start decades before symptoms. Over time, mutant stem cells outcompete healthy ones, reshaping the bone marrow. Donate to research: https://goto.mpnresearchfoundation.org/4js24x1 

#MPNResearch #FoundationForward #BloodHealth
May 20, 2025 at 1:01 AM
#NedWeinshanker shared this while reading @SuleikaJaouad book: “We were more than circumstantial friends. We were family.” 

It’s what Bob Rosen set out to build — a community where patients are partners. 

Join us: https://f.mtr.cool/lzvyigoolu 
 #FoundationForward #MPNResearch
May 14, 2025 at 5:01 PM
Today would’ve been our founder Bob Rosen’s 81st birthday. He turned his PV diagnosis into 25 years of impact. 

Honor his legacy by donating to move #FoundationForward. 

Every gift is matched up to $43K: https://f.mtr.cool/eaxbzwfcwv
May 7, 2025 at 5:04 PM
Our founder, Bob Rosen’s legacy lives on through 25 years of MPN research. 

$20M+ invested. 100+ projects funded.

Donate today — every gift matched up to $30K: https://f.mtr.cool/cmpbctbgkz  
 
#FoundationForward #MPNResearch
MPN May Campaign – Foundation Forward – MPN Research Foundation
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May 1, 2025 at 5:04 PM